Iolascon, A <br/><br/>
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis.  [electronic resource] 

 -  Blood  Feb 1998 
 - 1093 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Glucuronosyltransferase--genetics<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Polymorphism, Genetic<br/>Promoter Regions, Genetic<br/>Spherocytosis, Hereditary--genetics